MIR765
gene geneOn this page
Also known as hsa-mir-765
Summary
MIR765 (microRNA 765, HGNC:33141) is a microRNA gene on chromosome 1q23.1.
microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop.
Source: NCBI Gene 768220 — RefSeq curated summary.
At a glance
- Gene type: non-coding (miRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:33141 |
| Approved symbol | MIR765 |
| Name | microRNA 765 |
| Location | 1q23.1 |
| Locus type | RNA, micro |
| Status | Approved |
| Aliases | hsa-mir-765 |
| Ensembl gene | ENSG00000211581 |
| Ensembl biotype | miRNA |
| Entrez | 768220 |
| RNAcentral | URS000068E793 — miRNA, 114 nt, 2 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 miRNA
ENST00000390226
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000390226 — 1 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001507653 | 156936131 | 156936244 |
Expression profiles
Bgee: expression breadth ubiquitous, 111 present calls, max score 93.49.
Top tissues by expression
111 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| lower esophagus mucosa | UBERON:0035834 | 93.49 | gold quality |
| right uterine tube | UBERON:0001302 | 92.71 | gold quality |
| sural nerve | UBERON:0015488 | 87.12 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 84.94 | gold quality |
| prefrontal cortex | UBERON:0000451 | 84.82 | gold quality |
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 84.80 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 82.63 | gold quality |
| endocervix | UBERON:0000458 | 82.43 | gold quality |
| pituitary gland | UBERON:0000007 | 81.99 | gold quality |
| prostate gland | UBERON:0002367 | 81.30 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 81.14 | gold quality |
| urinary bladder | UBERON:0001255 | 81.11 | gold quality |
| fundus of stomach | UBERON:0001160 | 81.07 | gold quality |
| left uterine tube | UBERON:0001303 | 80.83 | gold quality |
| right coronary artery | UBERON:0001625 | 80.55 | gold quality |
| monocyte | CL:0000576 | 80.30 | gold quality |
| calcaneal tendon | UBERON:0003701 | 80.21 | gold quality |
| left testis | UBERON:0004533 | 80.14 | gold quality |
| right lobe of liver | UBERON:0001114 | 80.10 | gold quality |
| blood | UBERON:0000178 | 80.07 | gold quality |
| right testis | UBERON:0004534 | 79.98 | gold quality |
| vagina | UBERON:0000996 | 79.54 | gold quality |
| ectocervix | UBERON:0012249 | 79.50 | gold quality |
| adenohypophysis | UBERON:0002196 | 79.43 | gold quality |
| esophagogastric junction muscularis propria | UBERON:0035841 | 79.32 | gold quality |
| ascending aorta | UBERON:0001496 | 79.28 | gold quality |
| myometrium | UBERON:0001296 | 79.05 | gold quality |
| testis | UBERON:0000473 | 79.04 | gold quality |
| thoracic aorta | UBERON:0001515 | 78.92 | gold quality |
| liver | UBERON:0002107 | 78.78 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.23 |
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 22)
- Plasma levels of miR-765 and miR-149 might be used as noninvasive biomarkers for the diagnosis of CAD in geriatric people. (PMID:25664324)
- rs3115758 accounts for the susceptibility of arterial stiffening through miR-765-induced apelin repression. (PMID:25882991)
- EMP3 functions as an oncogene and is regulated by microRNA-765 in primary breast carcinoma. (PMID:26398721)
- miR-765 is a potential onco-miR that participates in carcinogenesis of human hepatocellular carcinoma by suppressing INPP4B expression, and might represent a potential therapeutic target for hepatocellular carcinoma patients. (PMID:27062697)
- Our results suggest a general role of miR-206,-381, and 671-5p in SMARCB1 gene silencing of epithelioid sarcomas(ES) , extraskeletal myxoid chondrosarcomas , malignant peripheral nerve sheath tumors and synovial sarcomas . In the future, miR-765 could possibly be a diagnostic tool for ES because of its 97% specificity and 80% sensitivity. (PMID:27223121)
- It regulates tumor development of tongue squamous cell carcinoma together with LINC00511 and LAMC2. (PMID:29315846)
- HOXB9 directly binds to the promoter of microRNA-765 and facilitates its transcription, which in turn targets FOXA2, resulting in a FOXA2 decrease and cancer stem cell increase. Elevated HOXB9 is found in human melanoma tissues, which is associated with microRNA-765 up-regulation and FOXA2 decreases. (PMID:29408459)
- that LINC00994 and RUNX2 are upregulated in pancreatic cancers as compared to non-cancer tissues, while miR-765-3p is downregulated. Silencing of LINC00994 inhibits the growth, migration and invasion, promotes a G1 cell cycle arrest and apoptosis in pancreatic cancer cells in vitro. (PMID:30739523)
- MicroRNA-765 targets MTUS1 to promote the progression of osteosarcoma via mediating ERK/EMT pathway. (PMID:31210288)
- Clinical value of LHPP-associated microRNAs combined with protein induced by vitamin K deficiency or antagonist-II in the diagnosis of alpha-fetoprotein-negative hepatocellular carcinoma. (PMID:31693242)
- MiR-765 functions as a tumour suppressor and eliminates lipids in clear cell renal cell carcinoma by downregulating PLP2. (PMID:31901870)
- miR-765 inhibits the osteogenic differentiation of human bone marrow mesenchymal stem cells by targeting BMP6 via regulating the BMP6/Smad1/5/9 signaling pathway. (PMID:32059748)
- miRNA-765 mediates multidrug resistance via targeting BATF2 in gastric cancer cells. (PMID:32166887)
- Bromodomain-containing protein 4 silencing by microRNA-765 produces anti-ovarian cancer cell activity. (PMID:33686960)
- CD45RO(-)CD8(+) T cell-derived exosomes restrict estrogen-driven endometrial cancer development via the ERbeta/miR-765/PLP2/Notch axis. (PMID:33859750)
- miR-765 targeting PDX1 impairs pancreatic beta-cell function to induce type 2 diabetes. (PMID:34357821)
- Three LHPP gene-targeting co-expressed microRNAs (microRNA-765, microRNA-21, and microRNA-144) promote proliferation, epithelial-mesenchymal transition, invasion, and are independent prognostic biomarkers in renal cell carcinomas patients. (PMID:34699621)
- lncRNA USP30-AS1 sponges miR-765 and modulates the progression of colon cancer. (PMID:35260141)
- TRG16, targeted by miR-765, inhibits breast cancer stem cell-like properties via regulating the NF-kappaB pathway. (PMID:35648115)
- Hsa_circ_0007478 aggravates NLRP3 inflammasome activation and lipid metabolism imbalance in ox-LDL-stimulated macrophage via miR-765/EFNA3 axis. (PMID:36191606)
- Long noncoding RNA long intergenic non-protein-coding RNA 173 contributes to nasopharyngeal carcinoma progression by regulating microRNA-765/Gremlin 1 pathway. (PMID:37365917)
- The role of miR-765 in human cancers. (PMID:39068750)
Cross-species orthologs
0 orthologs
Protein
Non-coding RNA — no protein product; not a drug target.
Function
No curated pathway, Gene-Ontology, or interaction data.
Disease & clinical
No curated disease, variant, or cancer-driver associations.
Drugs & pharmacology
No drug or pharmacology data — not an established drug target.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.